Epidermolysis bullosa
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Epidermolysis bullosa
Integumentary system
Keratotic skin disorders
Actinic keratosis
Papulosquamous and inflammatory skin disorders
Atopic dermatitis
Contact dermatitis
Lichen planus
Pityriasis rosea
Psoriasis
Seborrhoeic dermatitis
Urticaria
Skin infections
Cellulitis
Erysipelas
Impetigo
Necrotizing fasciitis
Candida
Malassezia (Tinea versicolor and Seborrhoeic dermatitis)
Pediculus humanus and Phthirus pubis (Lice)
Sarcoptes scabiei (Scabies)
Human herpesvirus 6 (Roseola)
Measles virus
Parvovirus B19
Rubella virus
Varicella zoster virus
Coxsackievirus
Herpes simplex virus
Human papillomavirus
Poxvirus (Smallpox and Molluscum contagiosum)
Varicella zoster virus
Integumentary system pathology review
Acneiform skin disorders: Pathology review
Bacterial and viral skin infections: Pathology review
Papulosquamous and inflammatory skin disorders: Pathology review
Pigmentation skin disorders: Pathology review
Skin cancer: Pathology review
Vesiculobullous and desquamating skin disorders: Pathology review
Viral exanthems of childhood: Pathology review
Assessments
Epidermolysis bullosa
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Epidermolysis bullosa
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Summary
Epidermolysis bullosa (EB) is a group of rare genetic skin disorders in which the skin is fragile and forms blisters easily after a minor trauma, especially in warm weather. There exists over 30 subtypes of EB, classified into major 4 groups based on the plane of cleavage within the skin and the underlying molecular defects. These are EB simplex, junctional EB, dystrophic EB and Kindler EB.
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